نتایج جستجو برای: gene polymorphism

تعداد نتایج: 1185940  

Arezoo Akmali, Hossein Dehghani, Khadije Shahrokhabadi,

Introduction: Considering the effectiveness of polymorphisms in the occurrence of respiratory diseases, it seems that these genetic variations in viral and microbial receptors can be effective in the occurrence and progression of the disease. The present study aimed to  assess the relationship between the C-159T polymorphism in the CD14 gene promoter and the severity of the disease in  Covid-19...

آذرفام, پروین, حسین‌پور فیضی, محمدعلی, حلیمی, منیژه, رجحان ن‍ژاد, مهدیه, منتظری, وحید, پولادی, ناصر,

Introduction: Survivin gene, as an apoptosis inhibitor, plays an important role in development of breast cancer. The differential expression of survivin in cancer versus normal adult cells as well as an association between high expression of survivin and aggressive tumors has led to use of survivin as a molecular marker for diagnosis and prognosis of tumors. The underlying mechanism of survivin...

Ahmadi-Sina Nedaei Ahmadi Mohammad Ali Ghayumi Nasrollah Erfani, Zahra Mojtahedi

Background: An association between lung cancer and chemokines has been advocated in the recent years. This study aims at investigating the association between lung cancer and 16C/A single nucleotide polymorphism (SNP) (rs. 4359426) in C-C motif chemokine 22 (CCL22) as well as C1014T SNP (rs. 2228428) in C-C chemokine receptor type 4 (CCR4), which serves as the receptor for CCL22.Methods: Genoty...

Journal: :genetics in the 3rd millennium 0
mahboobeh moghadaszadeh mohammmadreza mohammadabadi, ali esmailizadeh koshkoieh

the raini cashmere goat is one of the iranian goat breeds with a high economic value on international markets due to its high production and high quality. the bmp15 gene regulates granulose cell proliferation and differentiation by promoting granulosa cell mitosis, suppressing follicle-stimulating hormone receptor expression, and stimulating the kit ligand expression. this gene plays a pivotal ...

بنیادی, مرتضی, جبارپور بنیادی, محمدحسین, جوادزاده, علیرضا, محمدیان, طاهره,

Introduction & Objective: Age-related macular degeneration (AMD) is a disease affecting the central regions of the retina and choroid, which can lead to loss of central vision. Etiological research suggests that AMD is a complex disease, caused by the actions and interactions of multiple genes and environmental factors. Numerous studies have focused on the role of chemotactic cytokines, also kn...

J.N.P. Puoli Filho L.A.L. Chardulo L.C.M. Armeiro M.D. Silveira da Mota, R.A. Curi

The aims of the present study were to propose apolymerase chain reaction-restriction fragment length polymorphismPCR-RFLP genotyping method for the AY_376689:c.773C>T single nucleotide polymorphism SNP of the equine PRKAG3 gene, related to muscle performance, as well as to characterize this SNP and a second polymorphism, AAWR_02017454:g.121684T>C of the SPATA1 gene, related to male fertility, i...

ژورنال: یافته 2016
سروری, جمال, معطری, آفاق, نوروزیان, حسین,

Background: Hepatitis C virus (HCV) is a worldwide health problem, which associated with cirrhosis and hepatocellular carcinoma. Interferon-α and Ribavirin are only acceptable treatment regimen for these patients. These regimen are effective only on 50% of the patients. The aim of this study was to evaluate the response to treatment with interferon gamma gene polymorphism in patients with...

ژورنال: کومش 2020

Introduction: PGC-1α gene plays an important role in regulating cellular energy metabolism and stimulating the increased cell mitochondrial mass. Understanding the status of this gene polymorphism in non-athletic male adolescents may be helpful in choosing and identifying the sport talented male adolescents. The purpose of the present study was to investigate possible association between PGC-1α...

Journal: :Journal of advances in medical and biomedical research 2023

Single-Nucleotide Polymorphism of rs11061971 (+219 A>T) in Adiponectin Receptor 2 (AdipoR2) Gene and its Association with Risk Type Diabetes among Iranian Population

Fatemeh Hosseini Mohammadreza Bazrafshani Najmeh NezamabadiPour Saeedeh Parvaresh

Background & Aims: Vesicoureteral Reflux (VUR) is a congenital defect of the urinary tract which has been reported in approximately 1% of children. Several immunological and genetic factors are listed as major causes of this problem. The C825T polymorphism of the GNB3 gene is among the genetic factors that may be involved in the development or progression of the disease. Participatory role o...

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